CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 1,277 enrolled
Drug / intervention
Saliva test kitdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04568122
NCT04568122N/ACompleted

Rapid Turnaround, Home-based Saliva Testing for COVID-19

Stanford University·interventional·Posted Sep 29, 2020·Updated Jan 10, 2024

In Brief

A clinical study evaluating Saliva test kit for Covid19. Completed, enrolled 1,277 participants across 2 sites.

Detailed Summary

The aim of the study is to demonstrate the feasibility and validity of a saliva based home surveillance monitoring test for SARS-CoV-2 infection. Participants will be asked to carry out as many tests as are included in the bag they are provided, on a daily basis until they are used up.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCovid19
CountriesUnited States
CollaboratorsBioBox

Timeline

N/ACompletedFinished
202120222023202420252026
First PostedSep 29, 2020
Enrollment StartNov 20, 2020
Primary CompletionDec 10, 2022
TodayJul 2, 2026
Enrollment to primary: 2.1 yearsPosted 5.8 years ago

Interventions

Saliva test kitdevice

Kit including tube with closed reagents using loop-mediated isothermal amplification (LAMP) assay to detect SARS-CoV-2 virus.